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Nottingham Prognostic Index Plus (NPI+): a modern clinical decision making tool in breast cancer

BACKGROUND: Current management of breast cancer (BC) relies on risk stratification based on well-defined clinicopathologic factors. Global gene expression profiling studies have demonstrated that BC comprises distinct molecular classes with clinical relevance. In this study, we hypothesised that mol...

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Autores principales: Rakha, E A, Soria, D, Green, A R, Lemetre, C, Powe, D G, Nolan, C C, Garibaldi, J M, Ball, G, Ellis, I O
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974073/
https://www.ncbi.nlm.nih.gov/pubmed/24619074
http://dx.doi.org/10.1038/bjc.2014.120
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author Rakha, E A
Soria, D
Green, A R
Lemetre, C
Powe, D G
Nolan, C C
Garibaldi, J M
Ball, G
Ellis, I O
author_facet Rakha, E A
Soria, D
Green, A R
Lemetre, C
Powe, D G
Nolan, C C
Garibaldi, J M
Ball, G
Ellis, I O
author_sort Rakha, E A
collection PubMed
description BACKGROUND: Current management of breast cancer (BC) relies on risk stratification based on well-defined clinicopathologic factors. Global gene expression profiling studies have demonstrated that BC comprises distinct molecular classes with clinical relevance. In this study, we hypothesised that molecular features of BC are a key driver of tumour behaviour and when coupled with a novel and bespoke application of established clinicopathologic prognostic variables can predict both clinical outcome and relevant therapeutic options more accurately than existing methods. METHODS: In the current study, a comprehensive panel of biomarkers with relevance to BC was applied to a large and well-characterised series of BC, using immunohistochemistry and different multivariate clustering techniques, to identify the key molecular classes. Subsequently, each class was further stratified using a set of well-defined prognostic clinicopathologic variables. These variables were combined in formulae to prognostically stratify different molecular classes, collectively known as the Nottingham Prognostic Index Plus (NPI+). The NPI+ was then used to predict outcome in the different molecular classes. RESULTS: Seven core molecular classes were identified using a selective panel of 10 biomarkers. Incorporation of clinicopathologic variables in a second-stage analysis resulted in identification of distinct prognostic groups within each molecular class (NPI+). Outcome analysis showed that using the bespoke NPI formulae for each biological BC class provides improved patient outcome stratification superior to the traditional NPI. CONCLUSION: This study provides proof-of-principle evidence for the use of NPI+ in supporting improved individualised clinical decision making.
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spelling pubmed-39740732014-04-03 Nottingham Prognostic Index Plus (NPI+): a modern clinical decision making tool in breast cancer Rakha, E A Soria, D Green, A R Lemetre, C Powe, D G Nolan, C C Garibaldi, J M Ball, G Ellis, I O Br J Cancer Clinical Study BACKGROUND: Current management of breast cancer (BC) relies on risk stratification based on well-defined clinicopathologic factors. Global gene expression profiling studies have demonstrated that BC comprises distinct molecular classes with clinical relevance. In this study, we hypothesised that molecular features of BC are a key driver of tumour behaviour and when coupled with a novel and bespoke application of established clinicopathologic prognostic variables can predict both clinical outcome and relevant therapeutic options more accurately than existing methods. METHODS: In the current study, a comprehensive panel of biomarkers with relevance to BC was applied to a large and well-characterised series of BC, using immunohistochemistry and different multivariate clustering techniques, to identify the key molecular classes. Subsequently, each class was further stratified using a set of well-defined prognostic clinicopathologic variables. These variables were combined in formulae to prognostically stratify different molecular classes, collectively known as the Nottingham Prognostic Index Plus (NPI+). The NPI+ was then used to predict outcome in the different molecular classes. RESULTS: Seven core molecular classes were identified using a selective panel of 10 biomarkers. Incorporation of clinicopathologic variables in a second-stage analysis resulted in identification of distinct prognostic groups within each molecular class (NPI+). Outcome analysis showed that using the bespoke NPI formulae for each biological BC class provides improved patient outcome stratification superior to the traditional NPI. CONCLUSION: This study provides proof-of-principle evidence for the use of NPI+ in supporting improved individualised clinical decision making. Nature Publishing Group 2014-04-01 2014-03-11 /pmc/articles/PMC3974073/ /pubmed/24619074 http://dx.doi.org/10.1038/bjc.2014.120 Text en Copyright © 2014 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Clinical Study
Rakha, E A
Soria, D
Green, A R
Lemetre, C
Powe, D G
Nolan, C C
Garibaldi, J M
Ball, G
Ellis, I O
Nottingham Prognostic Index Plus (NPI+): a modern clinical decision making tool in breast cancer
title Nottingham Prognostic Index Plus (NPI+): a modern clinical decision making tool in breast cancer
title_full Nottingham Prognostic Index Plus (NPI+): a modern clinical decision making tool in breast cancer
title_fullStr Nottingham Prognostic Index Plus (NPI+): a modern clinical decision making tool in breast cancer
title_full_unstemmed Nottingham Prognostic Index Plus (NPI+): a modern clinical decision making tool in breast cancer
title_short Nottingham Prognostic Index Plus (NPI+): a modern clinical decision making tool in breast cancer
title_sort nottingham prognostic index plus (npi+): a modern clinical decision making tool in breast cancer
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974073/
https://www.ncbi.nlm.nih.gov/pubmed/24619074
http://dx.doi.org/10.1038/bjc.2014.120
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